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The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome

CD146, involved in epithelial-to-mesenchymal transition (EMT), might affect cancer aggressiveness. We here investigated the prevalence of CD146 expression in breast cancer subtypes, its relation to prognosis, the relation between CD146 and EMT and the outcome to tamoxifen. Primary breast cancer tiss...

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Autores principales: de Kruijff, Ingeborg E., Timmermans, Anna M., den Bakker, Michael A., Trapman-Jansen, Anita M.A.C., Foekens, Renée, Meijer-Van Gelder, Marion E., Oomen-de Hoop, Esther, Smid, Marcel, Hollestelle, Antoinette, van Deurzen, Carolien H.M., Foekens, John A., Martens, John W.M., Sleijfer, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977107/
https://www.ncbi.nlm.nih.gov/pubmed/29734758
http://dx.doi.org/10.3390/cancers10050134
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author de Kruijff, Ingeborg E.
Timmermans, Anna M.
den Bakker, Michael A.
Trapman-Jansen, Anita M.A.C.
Foekens, Renée
Meijer-Van Gelder, Marion E.
Oomen-de Hoop, Esther
Smid, Marcel
Hollestelle, Antoinette
van Deurzen, Carolien H.M.
Foekens, John A.
Martens, John W.M.
Sleijfer, Stefan
author_facet de Kruijff, Ingeborg E.
Timmermans, Anna M.
den Bakker, Michael A.
Trapman-Jansen, Anita M.A.C.
Foekens, Renée
Meijer-Van Gelder, Marion E.
Oomen-de Hoop, Esther
Smid, Marcel
Hollestelle, Antoinette
van Deurzen, Carolien H.M.
Foekens, John A.
Martens, John W.M.
Sleijfer, Stefan
author_sort de Kruijff, Ingeborg E.
collection PubMed
description CD146, involved in epithelial-to-mesenchymal transition (EMT), might affect cancer aggressiveness. We here investigated the prevalence of CD146 expression in breast cancer subtypes, its relation to prognosis, the relation between CD146 and EMT and the outcome to tamoxifen. Primary breast cancer tissues from 1342 patients were available for this retrospective study and immunohistochemically stained for CD146. For survival analyses, pure prognosis was studied by only including lymph-node negative patients who did not receive (neo)adjuvant systemic treatment (n = 551). 11% of the tumors showed CD146 expression. CD146 expression was most prevalent in triple-negative cases (64%, p < 0.001). In univariable analysis, CD146 expression was a prognostic factor for both metastasis-free survival (MFS) (p = 0.020) and overall survival (OS) (p = 0.037), but not in multivariable analysis (including age, tumor size, grade, estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) and Ki-67). No correlation between CD146 and EMT nor difference in outcome to first-line tamoxifen was seen. In this large series, our data showed that CD146 is present in primary breast cancer and is a pure prognostic factor for MFS and OS in breast cancer patients. We did not see an association between CD146 expression and EMT nor on outcome to tamoxifen.
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spelling pubmed-59771072018-05-31 The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome de Kruijff, Ingeborg E. Timmermans, Anna M. den Bakker, Michael A. Trapman-Jansen, Anita M.A.C. Foekens, Renée Meijer-Van Gelder, Marion E. Oomen-de Hoop, Esther Smid, Marcel Hollestelle, Antoinette van Deurzen, Carolien H.M. Foekens, John A. Martens, John W.M. Sleijfer, Stefan Cancers (Basel) Article CD146, involved in epithelial-to-mesenchymal transition (EMT), might affect cancer aggressiveness. We here investigated the prevalence of CD146 expression in breast cancer subtypes, its relation to prognosis, the relation between CD146 and EMT and the outcome to tamoxifen. Primary breast cancer tissues from 1342 patients were available for this retrospective study and immunohistochemically stained for CD146. For survival analyses, pure prognosis was studied by only including lymph-node negative patients who did not receive (neo)adjuvant systemic treatment (n = 551). 11% of the tumors showed CD146 expression. CD146 expression was most prevalent in triple-negative cases (64%, p < 0.001). In univariable analysis, CD146 expression was a prognostic factor for both metastasis-free survival (MFS) (p = 0.020) and overall survival (OS) (p = 0.037), but not in multivariable analysis (including age, tumor size, grade, estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) and Ki-67). No correlation between CD146 and EMT nor difference in outcome to first-line tamoxifen was seen. In this large series, our data showed that CD146 is present in primary breast cancer and is a pure prognostic factor for MFS and OS in breast cancer patients. We did not see an association between CD146 expression and EMT nor on outcome to tamoxifen. MDPI 2018-05-05 /pmc/articles/PMC5977107/ /pubmed/29734758 http://dx.doi.org/10.3390/cancers10050134 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
de Kruijff, Ingeborg E.
Timmermans, Anna M.
den Bakker, Michael A.
Trapman-Jansen, Anita M.A.C.
Foekens, Renée
Meijer-Van Gelder, Marion E.
Oomen-de Hoop, Esther
Smid, Marcel
Hollestelle, Antoinette
van Deurzen, Carolien H.M.
Foekens, John A.
Martens, John W.M.
Sleijfer, Stefan
The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome
title The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome
title_full The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome
title_fullStr The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome
title_full_unstemmed The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome
title_short The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome
title_sort prevalence of cd146 expression in breast cancer subtypes and its relation to outcome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977107/
https://www.ncbi.nlm.nih.gov/pubmed/29734758
http://dx.doi.org/10.3390/cancers10050134
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